plerixafor has been researched along with aspartic acid in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bridger, GJ; Gerlach, LO; Schwartz, TW; Skerlj, RT | 1 |
| Bridger, G; De Clercq, E; Gerlach, LO; Hatse, S; Henson, G; Princen, K; Schols, D; Schwartz, TW | 1 |
| Bridger, GJ; Gerlach, LO; Jakobsen, JS; Jensen, KP; Rosenkilde, MR; Ryde, U; Schwartz, TW; Skerlj, RT | 1 |
3 other study(ies) available for plerixafor and aspartic acid
| Article | Year |
|---|---|
Molecular interactions of cyclam and bicyclam non-peptide antagonists with the CXCR4 chemokine receptor.
Topics: Amino Acid Sequence; Animals; Anti-HIV Agents; Antiviral Agents; Asparagine; Aspartic Acid; Benzylamines; Binding, Competitive; Chemokine CXCL12; Chemokines, CXC; COS Cells; Cyclams; DNA, Complementary; Heterocyclic Compounds; Humans; Inhibitory Concentration 50; Kinetics; Ligands; Linear Models; Models, Chemical; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Binding; Protein Conformation; Receptors, CXCR4; Transfection | 2001 |
Mutation of Asp(171) and Asp(262) of the chemokine receptor CXCR4 impairs its coreceptor function for human immunodeficiency virus-1 entry and abrogates the antagonistic activity of AMD3100.
Topics: Amino Acid Sequence; Anti-HIV Agents; Aspartic Acid; Benzylamines; Cyclams; Heterocyclic Compounds; HIV-1; Humans; Molecular Sequence Data; Mutation; Receptors, Chemokine; Receptors, CXCR4; Receptors, Virus; Transfection; Tumor Cells, Cultured | 2001 |
Metal ion enhanced binding of AMD3100 to Asp262 in the CXCR4 receptor.
Topics: Amino Acid Sequence; Animals; Aspartic Acid; Benzylamines; Binding, Competitive; Carboxylic Acids; Cations, Divalent; Chemokine CXCL12; Chemokines, CXC; Copper; COS Cells; Cyclams; DNA Mutational Analysis; Heterocyclic Compounds; Humans; Ligands; Macromolecular Substances; Metals, Heavy; Molecular Sequence Data; Mutagenesis, Site-Directed; Nickel; Receptors, CXCR4; Transfection; Zinc | 2003 |